FDA label 2882401e-88ab-cf31-e063-6394a90a86c8

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
5bc8fe94-9469-4b6b-b271-cd6d1d9f8c4f
SPL ID
2882401e-88ab-cf31-e063-6394a90a86c8
Version
2
Effective date
2024-12-05
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:44:53

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Warnings: 1. Stop using the product if there is any of the following abnormal symptoms appeared after use and consult with your dermatologist as continued use can worsen the symptoms. A) if there are red spots, swelling, itchiness, or irritation B) if the above symptoms appear around the skin to which the product has been applied, after being exposed to direct sunlight. 2. Do not apply the product to any parts of the skin with wound, eczema, or dermatitis. 3. Precautions on storage and handling. A) Make sure to close the cap after use. B) Keep out of the reach of children and babies. C) Do not keep the product in a hot or cold place or a place getting direct sunlight.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.